The document discusses the resonance stabilization of a second phenol after hydrogen is removed from the hydroxyl group. It describes how the negative charge on the oxygen creates a series of double bond movements, eventually leading to a negative charge on the oxygen. This process involves interactions with nitrogen in the molecule.

1. The second phenol can resonance stabilize once the H has been removed from the
O. The negative charge on the O would come down and create a double bond, the other double
bond would move over counterclockwise, the next double bond will move towards the nitrogen,
and finally the double bond will go from the N-O bond onto the O, giving it a negative charge.
Solution
The second phenol can resonance stabilize once the H has been removed from the
O. The negative charge on the O would come down and create a double bond, the other double
bond would move over counterclockwise, the next double bond will move towards the nitrogen,
and finally the double bond will go from the N-O bond onto the O, giving it a negative charge.